# The impact of metabolic reprogramming in hepatocellular carcinoma on T cell

**Authors:** Dong-Xu Liao, Xiang An, Gui-Xiang Huang, Tong-Ling Yuan

PMC · DOI: 10.3389/fimmu.2025.1696113 · Frontiers in Immunology · 2025-11-10

## TL;DR

This paper reviews how changes in metabolism in liver cancer cells create an environment that weakens T cell immunity, and explores new treatment strategies to improve immunotherapy outcomes.

## Contribution

The paper highlights new insights into how metabolic changes in liver cancer suppress T cells and identifies potential targets for combination therapies.

## Key findings

- Metabolic reprogramming in HCC cells creates an immunosuppressive tumor environment.
- Nutrient competition and inhibitory metabolites are key to T cell suppression.
- Combining metabolic and immune-targeted therapies may improve HCC treatment.

## Abstract

Hepatocellular carcinoma (HCC) is the predominant type of liver cancer, characterized by high incidence and mortality rates. Despite advancements in surgical and systemic therapies, the prognosis remains poor due to the asymptomatic nature of early-stage HCC. Metabolic reprogramming in HCC cells usually creates an immunosuppressive tumor microenvironment (TME), thereby impeding T cell-mediated antitumor immunity. This review focuses on the metabolic reprogramming patterns in HCC, their impact on T cell function, and the potential of metabolic-immune targeted combination therapies. We emphasize that nutrient competition and the accumulation of inhibitory metabolites are key mechanisms underlying T cell suppression in the TME. This review provides an update on the complex metabolic-immune interactions and helps to identify new therapeutic targets to improve the efficacy of immunotherapy for HCC.

## Linked entities

- **Diseases:** Hepatocellular carcinoma (MONDO:0007256), HCC (MONDO:0007256)

## Full-text entities

- **Diseases:** tumor (MESH:D009369), HCC (MESH:D006528)

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12640927/full.md

## References

337 references — full list in the complete paper: https://tomesphere.com/paper/PMC12640927/full.md

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Source: https://tomesphere.com/paper/PMC12640927